Pigments

ABSTRACT

Pigments of the general formula FxHet(I) where F is the cation of a cationic dye which has an absorption maximum at &gt;700 nm and may or may not contain anionic groups and Het is an anion of a heteropolyacid based on tungsten, molybdenum, vanadium or a mixture of these with phosphorus, silicon, cobalt, aluminum, manganese, chromium, nickel or a mixture of these or a copper(I)-hexacyanoferrate(II) anion, are superior to the known IR dyes in terms of thermal stability and photostability, and give optical recording media having superior properties, such as a high signal/noise ratio.

This is a division of application Ser. No. 870,749, filed June 4, 1986,now U.S. Pat. No. 4,785,088.

Many known organic substances absorb in the long wavelength visiblespectral range and in the near IR range.

For a number of applications, many of these substances have thedisadvantage that their morphology cannot be maintained or modified inthe required manner, or the substances themselves are modified in anundesirable manner before, during and/or after processing, for exampleas a result of crystallization, fading due to light or heat, bleeding orchalking.

It is an object of the present invention to provide novel pigments whichabsorb at above 700 nm and do not have the disadvantages of the priorart IR-absorbing compounds.

We have found that this object is achieved by the pigments according tothe invention.

The present invention accordingly relates to pigments of the generalformula

    F·Het                                             (I)

where F is a cation of a cationic dye which has an absorptionmaximum >700 nm and may or may not contain anionic groups, and Het is ananion of a heteropolyacid based on tungsten and/or molybdenum withphosphorus, silicon, vanadium , cobalt, aluminum, manganese, chromiumand/or nickel or a copper(I)-hexacyanoferrate(II) anion [Cu₃ Fe(CN)₆].sup.⊖, the pigments being obtainable by laking the cationic dyes withthe heteropolyacids.

The novel pigments consist of uniform fine particles having a diameterof from about 10 to 1000 nm, depending on the preparation.

Many disadvantages of the soluble dyes can be overcome with the aid ofthe color lakes of the present invention.

The novel pigments (I) can easily be incorporated into polymers, and thelatter can be pigmented in the form of a solution or in the melt. Thepigments can also be incorporated into polymers by using dispersions of(I), and the pigments can be homogeneously distributed in a highconcentration. The color lakes (I) can be applied onto surfaces byconventional methods and can also be processed by conventional printingmethods, such as letterpress, gravure or offset printing. For example,bar codes which can be read using IR light sources can be produced byprinting.

The dispersions of the pigments (I) can also be used as an absorberlayer in optical storage media.

The pigments according to the present invention can furthermore beemployed for IR absorption in plastics or as an absorber layer in solarcollectors.

For certain applications, films containing (I) can also be used forsignal control by photodiodes emitting in the long wavelength range, forexample for switching off at the end of video and audio tapes.

Particularly suitable pigments (I) are those in which the dye cation Fis of the general formulae (II) to (VII): ##STR1##

In the formulae, R¹ and R² independently of one another are each C₁ -C₄-alkyl or are each heteroaryl or phenyl which is unsubstituted orsubstituted by hydroxyl, C₁ -C₄ -alkyl, C₁ -C₄ -alkoxy or halogen, X isoxygen or sulfur, Z is --(CH₂ --)_(r), where r is 2 or 3, T is phenyl orhalogen, such as bromine or chlorine, preferably phenyl or chlorine, oneof the radicals R³ and R⁴ is ##STR2## the other radicals R³ and R⁴,independently of one another, are each phenyl which is unsubstituted orsubstituted by C₁ -C₄ -alkyl, C₁ -C₄ -alkoxy or halogen or, in the4-position, by ##STR3## R⁵ and R⁶ independently of one another are eachhydrogen, C₁ -C₆ -alkyl, C₂ -C₆ -hydroxyalkyl, C₁ -C₄ -alkoxy-C₂ - or--C₃ -alkyl, allyl, 2-(C₂ -C₄ -alkanoyloxy)-ethyl or 2-cyanoethyl, or##STR4## is a radical of a saturated 5-membered or 6-memberedheterocyclic ring, Y is hydrogen, hydroxyl, C₁ -C₄ -alkyl or C₁ -C₄-alkoxy, m, n and q are each 0, 1 or 2, Pc is a (p+s+v) valent radicalof a metal-free phthalocyanine or of a metal phthalocyanine whichcontains VO, TiO, Pb, Sn, Cu, Ni or Mn as the central metal atom and inwhich the methylene group is bonded to a carbon atom of the imidazolering, p is 1 to 4, s is 0 or 1, v is 0, 1, 2, 3 or 4, Pc' is a w valentradical of a metal-free phthalocyanine or of a metal phthalocyanine whchcontains VO, TiO, Pb, Sn, Cu, Ni or Mn as the central metal, Hal isbromine, preferably chlorine or fluorine, R⁷ is C₁ -C₄ -alkyl, C₂ -C₄-hydroxyalkyl or C₂ -C₄ -aminoalkyl and w is 1, 2, 3 or 4.

Specific examples of radicals are as follows:

Halogen is fluorine, bromine and, in particular chlorine.

R¹ and R² are C₁ -C₄ -alkyl, such as methyl, ethyl, propyl and butyl,phenyl, 2-, 3- and 4-tolyl, 2-, 3- and 4-ethylphenyl, 3- and 4-n- and-isopropylphenyl, 3- and 4-n-, -iso- and -tert-butylphenyl, 2-, 3- and4-chlorophenyl, 3- and 4-bromophenyl, 3- and 4-methoxyphenyl, and 3- and4-ethoxyphenyl, of which the phenyl radicals substituted in the4-position are preferred; and hetaryl, such as 2- and 3-thienyl,4-thiazolyl and 2- and 3-furanyl. T is phenyl, chlorine or bromine,preferably phenyl or chlorine, Z is --CH₂ --₂ and --CH₂ --₃.

The remaining substituted phenyl radicals R³ and R⁴ are the substitutedphenyl radicals stated for R¹ and R², as well as phenyl which isunsubstituted and substituted in the 4-position by ##STR5##

R⁵ and R⁶ are each hydrogen, C₁ -C₆ -alkyl, such as methyl, ethyl, n-and isopropyl, n- and isobutyl, pentyl and n-hexyl, C₂ -C₄-hydroxyalkyl, such as 2-hydroxyethyl and 2- and 3-hydroxypropyl, C₁ -C₄-alkoxy-C₂ - or -C₃ -alkyl, such as 2-methoxyethyl, 2-ethoxyethyl, 2-n-and 2-isopropoxyethyl, 2-n-butoxyethyl, 3-methoxypropyl, 3-ethoxypropyl,3-n- and isopropoxypropyl and 3-n-butoxypropyl, allyl, 2-(C₂ -C₄-alkanoyloxy)-ethyl, such as 2-acetoxyethyl, 2-propionoxyethyl and2-butyryloxyethyl, and 2-cyanoethyl.

Furthermore, suitable radicals ##STR6## are radicals of saturated5-membered or 6-membered heterocyclic rings, such as pyrrolidinyl,piperidyl, morpholinyl, thiomorpholinyl, piperazinyl and N'-C₁ -C₄-alkylpiperazinyl, such as N'-methyl-, N'-ethyl- andN'-butylpiperazinyl.

Y is hydrogen, hydroxyl, C₁ -C₄ -alkyl, such as methyl, ethyl, n- andisopropyl, n-, iso- and tertbutyl, and C₁ -C₄ -alkoxy, such as methoxy,ethoxy, n- and isopropoxy and n-butoxy.

R⁷ is C₁ -C₄ -alkyl, such as methyl, ethyl, propyl and n- and isobutyl,C₂ -C₄ -hydroxyalkyl and C₂ -C₄ -aminoalkyl, such as 2-hydroxyethyl, 2-and 3-hydroxypropyl, 2-, 3- and 4-hydroxybutyl, 2-aminoethyl, 2- and3-aminopropyl and 4-aminobutyl.

Preferred pigments (I) are those which contain cations of the formulae(II), (IV), (VI) or (VII), where R¹ and R² are each phenyl, C₁ -C₄-alkylphenyl, C₁ -C₄ -alkoxyphenyl, 4-hydroxyphenyl, 2-thienyl ormethyl, m is 1 or 2, R³ and R⁴ are each ##STR7## and one of the 4radicals R³ and R⁴ may furthermore be phenyl, the radicals R¹⁰independently of one another are each C₁ -C₄ -alkyl, in particularmethyl or ethyl, q is 1 or 2, Pc is a metal phthalocyanine radicalcontaining VO, Pb, Mn or Sn as the central atom, p is 1, 2, 3 or 4, s is0, Hal is fluorine, v is 0 or 4, Pc' is a w-valent metal phthalocyanineradical containing VO, Pb, Mn or Sn as the central atom, R⁷ is C₁ -C₄-alkyl, 2-hydroxyethyl or 2-aminoethyl and w is 4.

Particularly noteworthy pigments (I) are those in which F is one of thefollowing cations:

    ______________________________________                                         ##STR8##                     (X)                                             Cation                                                                              R.sup.1         R.sup.2         m                                       ______________________________________                                        X.1                                                                                  ##STR9##                                                                                      ##STR10##      1                                       X.2                                                                                  ##STR11##                                                                                     ##STR12##      2                                       X.3                                                                                  ##STR13##                                                                                     ##STR14##      1                                       X.4   "               "               2                                       X.5                                                                                  ##STR15##                                                                                     ##STR16##      1                                       X.6   "               "               2                                       X.7                                                                                  ##STR17##                                                                                     ##STR18##      1                                       X.8   "               "               2                                       X.9   CH.sub.3        CH.sub.3        1                                       X.10  CH.sub.3         CH.sub.3       2                                       ______________________________________                                    

    ______________________________________                                         ##STR19##                    (XI)                                            Cation                                                                              R.sup.1         R.sup.2         m                                       ______________________________________                                        XI.1                                                                                 ##STR20##                                                                                     ##STR21##      1                                       XI.2                                                                                 ##STR22##                                                                                     ##STR23##      2                                       XI.3                                                                                 ##STR24##                                                                                     ##STR25##      1                                       XI.4  "               "               2                                       XI.5                                                                                 ##STR26##                                                                                     ##STR27##      1                                       XI.6  "               "               2                                       XI.7                                                                                 ##STR28##                                                                                     ##STR29##      1                                       XI.8  "               "               2                                       XI.9  CH.sub.3        CH.sub.3        1                                       XI.10 CH.sub.3        CH.sub.3        2                                       ______________________________________                                    

    ______________________________________                                         ##STR30##                   (XII)                                            Cation R.sup.1 = R.sup.2                                                                            Z          T                                            ______________________________________                                        XII.1                                                                                 ##STR31##     (CH.sub.2 ) .sub.2                                                                       Cl                                           XII.2                                                                                 ##STR32##     (CH.sub.2 ) .sub.2                                                                        ##STR33##                                   XII.3                                                                                 ##STR34##     (CH.sub.2 ) .sub.3                                                                       Cl                                           XII.4                                                                                 ##STR35##     (CH.sub.2 ) .sub.3                                                                        ##STR36##                                   XII.5  CH.sub.3       (CH.sub.2 ) .sub.2                                                                       Cl                                           XII.6  CH.sub.3       (CH.sub.2 ) .sub.2                                                                        ##STR37##                                   XII.7  CH.sub.3       (CH.sub.2 ) .sub.3                                                                       Cl                                           XII.8  CH.sub.3       (CH.sub.2 ) .sub.3                                                                        ##STR38##                                   XII.9                                                                                 ##STR39##     (CH.sub.2).sub.3                                                                         Cl                                           XII.10                                                                                ##STR40##     (CH.sub.2).sub.3                                                                          ##STR41##                                   ______________________________________                                    

    ______________________________________                                         ##STR42##                   (XIII)                                           Cation R.sup.1 = R.sup.2                                                                            Z          T                                            ______________________________________                                        XIII.1                                                                                ##STR43##     (CH.sub.2 ) .sub.2                                                                       Cl                                           XIII.2                                                                                ##STR44##     (CH.sub.2 ) .sub.2                                                                        ##STR45##                                   XIII.3                                                                                ##STR46##     (CH.sub.2 ) .sub.3                                                                       Cl                                           XIII.4                                                                                ##STR47##     (CH.sub.2 ) .sub.3                                                                        ##STR48##                                   XIII.5 CH.sub.3       (CH.sub.2 ) .sub.2                                                                       Cl                                           XIII.6 CH.sub.3       (CH.sub.2 ) .sub.2                                                                        ##STR49##                                   XIII.7 CH.sub.3       (CH.sub.2 ) .sub.3                                                                       Cl                                           XIII.8 CH.sub.3       (CH.sub.2 ) .sub.3                                                                        ##STR50##                                   XIII.9                                                                                ##STR51##     (CH.sub.2).sub.3                                                                         Cl                                           XIII.10                                                                               ##STR52##     (CH.sub.2).sub.3                                                                          ##STR53##                                   ______________________________________                                    

    ______________________________________                                         ##STR54##                   (XIV)                                            Cation     R.sup.12     R.sup.13   q                                          ______________________________________                                        XIV.1      N(CH.sub.3).sub.2                                                                          N(CH.sub.3).sub.2                                                                        1                                          XIV.2      N(CH.sub.3).sub.2                                                                          H          1                                          XIV.3      N(C.sub.2 H.sub.5).sub.2                                                                   N(C.sub.2 H.sub.5).sub.2                                                                 1                                          XIV.4      N(C.sub.2 H.sub.5).sub.2                                                                   H          1                                          XIV.5      NHC.sub.2 H.sub.5                                                                          NHC.sub.2 H.sub.5                                                                        1                                          XIV.6      NHC.sub.2 H.sub.5                                                                          H          1                                          XIV.7      N(CH.sub.3).sub.2                                                                          N(CH.sub.3).sub.2                                                                        2                                          XIV.8      N(CH.sub.2 H.sub.5).sub.2                                                                  N(C.sub.2 H.sub.5).sub.2                                                                 2                                          ______________________________________                                    

    ______________________________________                                         ##STR55##                    (XV)                                             Cation                                                                                    ##STR56##         R.sup.14                                       ______________________________________                                        XV.1        N(CH.sub.3).sub.2 N                                               XV.2        N(C.sub.2 H.sub.5).sub.2                                                                        H                                               XV.3                                                                                       ##STR57##        H                                               XV.4                                                                                       ##STR58##        H                                               XV.5                                                                                       ##STR59##        H                                               XV.6        N(C.sub.2 H.sub.5).sub.2                                                                        OH                                              XV.7        N(CH.sub.3).sub.2 OH                                              XV.8                                                                                       ##STR60##        OH                                              XV.9                                                                                       ##STR61##        OH                                              XV.10                                                                                      ##STR62##        OH                                              ______________________________________                                    

    ______________________________________                                         ##STR63##                   (XVI)                                            Cation  Pc           p     s      Hal  v                                      ______________________________________                                        XVI.1   VOPhth       1     0      --   0                                      XVI.2   VOPhth       2     0      --   0                                      XVI.3   MnPhth       1     0      --   0                                      XVI.4   MnPhth       2     0      --   0                                      XVI.5   PbPhth       2     0      --   0                                      XVI.6   PbPhth       1     0      --   0                                      XVI.7   SnPhth       1     0      --   0                                      XVI.8   SnPhth       2     0      --   0                                      XVI.9   VOPhth       1     0      F    4                                      XVI.10  VOPhth       2     0      F    4                                      ______________________________________                                    

    ______________________________________                                         ##STR64##                   (XVII)                                           Cation  Pc          R              w                                          ______________________________________                                        XVII.1  VOPhth      CH.sub.3       4                                          XVII.2  VOPhth      C.sub.2 H.sub.5                                                                              4                                          XVII.3  VOPhth      CH.sub.2 CH.sub.2 OH                                                                         4                                          XVII.4  VOPhth      CH.sub.2 CH.sub.2 NH.sub.2                                                                   4                                          ______________________________________                                    

The cationic dyes containing F are known or can be prepared by a knownmethod.

Suitable anions Het are derived from heteropolyacids based on tungsten,molybdenum or vanadium or mixtures of these with phosphorus, silicon,cobalt, aluminum, manganese, chromium or nickel or mixtures of these.The heteropolyacids of tungsten, of molybdenum, and of molybdenum andtungsten with phosphorus, silicon and/or vanadium are preferred. Thecopper (I)-hexacyano-ferrate(II) anion is also suitable.

The preparation of the heteropolyacids and of the salts of these acidsis known. The acids are obtained by acidifying solutions of tungstates,molybdates and/or vanadates in the form of the alkali metal and/orammonium salts in the presence of phosphate and/or water-solublesilicates. By selecting the ratios of tungstate, molybdate, vanadate andphosphate and/or silica or of their salts, it is possible to synthesizevarious heteropolyacids. Examples of heteropolyacids are phosphomolybdicacid, silicomolybdic acid, phosphotungstic acid, silicotungstic acid,phosphovanadic acid, silicovanadic acid, phosphotungstomolybdic acid,silicotungstomolybdic acid, phospho- and silicotungstovanadic acid andphosphosilicotungstomolybdic acid, which may furthermore containvanadium.

Phosphomolybdic acid, silicomolybdic acid, phosphotungstomolybdic acidand silicotungstomolybdic acid are preferred. The pigments (I) areprepared by a conventional method in which the cationic dyes containingF as a cation are laked with the heteropolyacids.

In order to obtain pigments which have a softer texture or more readilydispersible pigments, the aqueous filter cake can be converted to a drypowder by freeze-drying.

Another method comprises coating the precipitated pigments in aqueoussuspension with an emulsion of oleic acid ethanolamide and C₁₃ /C₁₅-paraffins in water or in the presence of aliphatic amines of not lessthan 10 carbon atoms, of long-chain alkylaminoalkanoic acids, of acidicor neutral phosphates, sulfuric acid half esters, long-chain alkanoicand alkenoic acids, alkylbenzenesulfonic acids, or adducts of ethyleneoxide with alkylphenols, with long-chain alkanols or with alkylamines,polypropylene/polyethylene block copolymers or alkylphenols (GermanLaid-Open Application DOS 3,435,433).

Where (I) is processed to printing inks containing nitrocellulose as abinder, the stability can be increased by adding compounds which contain--N(--CH₂ COOH)₂ groups, for example nitrilotriacetic acid ordiethylenediaminetetracetic acid (German Laid-Open Application DOS2,707,972).

The Examples which follow illustrate the preparation of the novelpigments.

The pigments which are obtained by laking and are isolated can be useddirectly.

It is a further object of the present invention to provide alight-absorbing layer for optical recording media which meets therequirements set for such layers and is simple to prepare, stable over along period, free from corrosion and non-toxic. Moreover, theserecording media should be capable of being read and written on by meansof a laser, such as an He-Ne laser or, preferably, a semiconductorlaser.

We have found that this object is achieved and that superior opticalrecording media are obtained, if the latter contain one or more pigmentsof the formula (I) in the light-absorbing layer.

The pigments used according to the invention can be applied as adispersion in a conventional manner, by immersion, knife-coating,spraying or whirler coating or by one of the conventional printingprocesses.

The recording media containing (I) have a high absorption atwavelengths >700 nm. These layers do not undergo troublesome changes, incontrast to layers which contain dyes in a molecular disperse (ie.dissolved) state. The novel layers do not crystallize and are stable tolight, environmental effects such as light and humidity, and elevatedtemperatures. Because of their high absorption, the novel recordingmedia are very sensitive to light from semiconductor lasers emitting atwavelengths of 750-900 nm.

The composition of the recording media is known per se and is part ofthe prior art (cf. for example U.S. Pat. Nos. 4,079,895, 4,242,689,4,241,355, 4,023,185 and 4,380,769; German Laid-Open Applications DOS3,007,296 and DOS 3,014,677; Japanese Preliminary Published Applications1 12 793/1983, 1 32 231/1983, 1 12 790/1983, 1 25 246/1983 and 56892/1983; and EP-A 84 729).

Examples of suitable bases are disks/plates which may or may not beprovided with a reflective coating and are made of glass or plastic,such as polymethyl methacrylate, polystyrene or polycarbonate, or ofmetal, such as aluminum.

A reflecting layer may be present underneath the light-absorbing layer,so that the incident light traveling through the colored layer (thelight which is not absorbed) is reflected by the reflector layer andagain travels through the colored layer.

Exposure can be effected through a transparent substrate. In this case,the sequence of layers is substrate-absorber layer-reflector; thereflector may be omitted.

According to the prior art (Bell, Spong; IEEE J. of Quantum ElectronicsVol. QE-14 (1978), 7, page 490; RCA Reviews 40 (1979), page 345), it isadvantageous if the thickness is equal to 1/4 of the wavelength of theincident light, since interference results in a particularly high levelof utilization (attenuation) of the incident light. However, we havefound that very sensitive recording media are also obtained with layerthicknesses which are substantially smaller than 1/4 of the wavelengthof the incident light.

The light-reflecting layer should be such that it very quantitativelyreflects the light used for recording and for scanning. Examples ofsuitable light-reflecting materials are aluminum, rhodium, gold,titanium, tin, lead, bismuth, copper and dielectric mirrors. Thethickness of the light-reflecting layer should be such that it reflectsas completely as possible the light used for recording or for scanning.

Reflecting materials having a low thermal conductivity are advantageousfor this purpose.

Bases, or the light-reflecting layer, must have an optically smooth,level surface, and the surface must be such that the absorbing layeradheres firmly to it.

Preferred pigments (I) are those of the formula (II), (IV), (VI) or(VII). These pigments have a high absorption in the range from about 700to 880 nm.

The pigments (I) are milled in a solvent which may or may not contain abinder, and are applied onto the base in the form of the resultingdispersion, by hirler-coating, knife-coating or immersion.

Any reflecting layers required are advantageously applied by vapordeposition under reduced pressure. Depending on the structure of thesystem, the reflecting layer is applied onto the base or onto theabsorbing layer. If appropriate, the reflecting layer may also bedispensed with. Suitable solvents or organic liquids for the dispersionare readily removable ones, such as methylene chloride, chloroform,acetone, methyl ethyl ketone, cyclohexane, toluene, acetonitrile, ethylacetate, methanol or mixtures of these. Examples of binders, which mayor may not be used, are polystyrene, polyvinyl acetate andpolyvinylprrolidone.

For writing, a modulated laser beam is used. As a result of absorptionof the incident light, the medium is heated at the appropriate point.Delamination processes, melting and/or vaporization processes produce achange in the reflectivity with respect to laser light at this point.

The conventional printing processes, such as letterpress, gravure,offset or screen printing, in particular offset printing and screenprinting, are very useful for applying the pigments (I) onto the bases.These printing processes can be used to produce non-erasable audio andvideo media. To do this, a dispersion (ink) whch contains one or morepigments (I) is used to print a pattern containing the storedinformation onto a base, for example an aluminum plate. The printedinformation can be read in a conventional manner by means of a laser,preferably a semiconductor laser, the laser beam being poorly reflectedby the printed areas and strongly reflected by the unprinted areas.

These processes are simple and economical and permit precisereproducibility. They give recording materials which are highly stableand have a long life and are therefore particularly useful for the massproduction of audio media (disks).

The Examples which follow illustrate the invention. Parts andpercentages are by weight.

A. PIGMENTS Example 1

10 parts of the dye XIV.1, in the form of the iodide, were dissolved in330 parts of 90% strength acetic acid under reflux, and the solution wasthen diluted with 400 parts of water. The dye was laked at 70° C. byadding a phosomolybdic acid solution prepared in a conventional mannerfrom 10.4 g of molybdenum oxide and 1.0 part of disodium phosphate in210 parts of water and having a pH of 2.2.

The pigment was stirred for a further 0.5 hour at 70° C. and thenfiltered off, wshed and dried at 75° C.

Example 2

The procedure described in Example 1 was followed, except that, beforethe laking process, the heteropolyacid obtained from 18.3 parts ofmolybdenum oxide and 1.76 parts of disodium phosphate in 230 parts ofwater was reduced with 4.4 parts of disodium sulfite and brought to pH1.0 with hydrochloric acid.

Example 3

The procedure described in Example 1 was followed except that, insteadof the phosphomolybdic acid, a heteropolyacid prepared in a conventionalmanner from 14.4 g of molybdenum oxide and 0.6 part of silica in 290parts of water and having a pH of 1 was used.

Example 4

The procedure described in Example 1 was followed, except that, insteadof the phosphomolybdic acid, a heteropolyacid prepared in a conventionalmanner from 3.25 parts of molybdenum oxide, 5.8 parts of tungsten oxideand 0.7-part of disodium phosphate and 140 parts of water and having apH of 2.2 was used.

Example 5

The procedure described in Example 1 was followed, except that, insteadof the phosphomolybdic acid, a heteropolyacid prepared in a conventionalmanner from 7.25 parts of molybdenum oxide, 11.6 parts of tungsten oxideand 0.63 part of silica in 230 parts of water and having a pH of 3.0 wasused.

Example 6

11.4 parts of dye XVI.2 were dissolved in 200 parts of 50% strengthacetic acid at 70° C., and was laked at this temperature with aheteropolyacid prepared in a conventional manner from 5.8 parts ofmolybdenum oxide and 0.56 part of disodium phosphate and 73 parts ofwater, reduced with 1.4 parts of Na₂ SO₃ and brought to pH 1.0 withhydrochloric acid.

The pigment was filtered off, washed and dried at 75° C.

Examples 7 to 33

The procedure described in Example 1, 2, 3, 4 or 5 was followed, exceptthat 10 parts of the dye stated in the Table were used.

    ______________________________________                                        Example   Dye cation                                                                              Counter ion from Example No.                              ______________________________________                                        8         X.1       1                                                         9         X.3       1                                                         10        X.7       1                                                         11        X.9       2                                                         12        XI.1      3                                                         13        XI.3      4                                                         14        XII.1     5                                                         15        XII.3     4                                                         16        XII.9     4                                                         17        XIII.3    5                                                         18        XIV.1     3                                                         19        XIV.3     1                                                         20        XIV.4     1                                                         21        XIV.7     2                                                         22        XIV.8     3                                                         23        XV.1      3                                                         24        XV.2      2                                                         25        XV.4      5                                                         26        XV.6      5                                                         27        XV.7      4                                                         28        XV.9      3                                                         29        XV.10     2                                                         30        XVI.2     2                                                         31        XVI.5     2                                                         32        XVII.1    1                                                         33        XVII.2    1                                                         ______________________________________                                    

B. RECORDING MEDIA Example 1 of Use

The dispersion described below was applied, by whirler coating, onto thereflector layer of a glass plate possessing a 50 nm thick aluminumreflector layer applied by vapor deposition. The layer was dried firstin the air and then under reduced pressure.

The dispersion was prepared as follows: 0.1 g of the pigment, preparedas described in Example 1 using the dye XIV.1 in the form of the iodide,and 0.2 g of polyvinyl acetate were milled in 15 ml of methyl ethylketone to give a dispersion.

Compared with the coatings containing molecular disperse cationic dyes,such as XIV.1 (counter ions: ClO₄ θ, BF₄ θ and CF₃ CO₂ θ), layerscontaining the corresponding laked dyes possess substantially higherthermal stability and in particular light stability. Furthermore, thelatter layers do not exhibit any change in morphology, such ascrystallization of chalking.

The recording medium obtained was irradiated (written on) by means oflight pulses from a semiconductor laser (820 nm), the intensity being 60mW and the pulse length 100 nsec, and the radiation being focussed to afocal point of 1.0 μm diameter on the surface of the dye layer.

For playback, a non-modulated semiconductor laser beam which wasfocussed in the same manner and attenuated to 1 mW by means of filterswas guided over the inscribed areas of the recording medium, and thelight reflected by the medium was measured using a photodetector. Owingto the change in the layer, the reflectance in an area whch has beenwritten on beforehand differs substantially from that of an area whichhas not been written on, and this can be determined at this point by thephotodetector.

Despite being substantially more stable to light and heat, the layercontaining XIV.1 in laked form is no less sensitive than layers whichcontain the corresponding molecular disperse dye.

Example 2 of Use

An aluminum reflector layer 50 nm thick was applied by vapor depositiononto a PMMA plate in a vacuum apparatus. A suspension of 0.1 g of thepigment which contains (X.3) as the cation and contains a counter ion asdescribed in Example 3, in a solution of 0.2 g of polyvinyl acetate in20 g of methyl ethyl ketone, was applied onto the PMMA base providedwith the reflective layer, and the dye layer was dried in the air andthen under reduced pressure at room temperature.

Like the recording medium of Example 1 of use, the resulting recordingmedium could be written on using a semiconductor laser (820 nm).

Examples 3 to 18 of Use

The procedure described in Example 2 of use was followed, and a pigmentdispersion was applied by whirler coating onto a PMMA plate providedwith a reflective aluminum layer about 50 nm thick.

The following pigments were used:

    ______________________________________                                        Example Pigment (I) with cation                                                                       Counter ion from Example                              ______________________________________                                        3       XIV.1           4                                                     4       XIV.3           1                                                     5       XIV.7           2                                                     6       X.3             5                                                     7       X.7             1                                                     8       XII.1           2                                                     9       X.1             3                                                     10      XII.3           4                                                     11      XII.9           5                                                     12      XI.1            2                                                     13      XI.1            5                                                     14      XV.1            1                                                     15      XV.6            2                                                     16      XVI.2           4                                                     17      XVII.2          4                                                     18      XVII.1          5                                                     ______________________________________                                    

We claim:
 1. A pigment of the formula:

    F.Het

where F is a dye cation of the formula: ##STR65## wherein R¹ and R²independently of one another are each C₁₋₄ -alkyl or are each 2- or3-thienyl, 4-thiazolyl or 2- or 3-furanyl or phenyl which isunsubstituted or substituted by hydroxyl, C₁₋₄ -alkyl, C₁₋₄ -alkoxy orbromine, chlorine or fluorine, X is oxygen or sulfur, Z is --(CH₂--)_(r), where r is 2 or 3, T is phenyl, chlorine or bromine, one of theradicals R³ and R⁴ is ##STR66## the other radicals R³ and R⁴,independently of one another, are each phenyl which is unsubstituted orsubstituted by C₁₋₄ -alkyl, C₁₋₄ -alkoxy or bromine, chlorine orfluorine or, in the 4-position by ##STR67## R⁵ and R⁶ independently ofone another are each hydrogen, C₁₋₆ -alkyl, C₂₋₆ -hydroxyalkyl, C₁₋₄-alkoxy-C₂ - or -C₃ -alkyl, allyl, 2-(C₂ -C₄ -alkanoyloxy)-ethyl or2-cyanoethyl, or ##STR68## is a pyrrolidinyl, piperidyl, morpholinyl,thiomorpholinyl, piperazinyl or N'-C₁₋₄ -alkylpiperazinyl, and m, n andq are each 0, 1 or 2, said cation having an absorption maximum ofgreater than 700 nm which may or may not contain anionic groups, and Hetis an anion of a heteropolyacid based on tungsten, molybdenum, vanadiumor a mixture of these with phosphorus, silicon, cobalt, aluminum,manganese, chromium, nickel or a mixture of these or is [Cu₃ Fe(CN)₆ ]⁻,the pigment being obtained by lacking the corresponding cationic dyewith the heteropolyacid.
 2. The pigment is claimed in claim 1, whereinHet is an anion of phosphomolybdic acid, of silicomolybdic acid, orphosphotungstomolybdic acid or of silicotungstomolybidc acid.
 3. Thepigment as claimed in claim 1, wherein F is a dye cation of the formula:##STR69## wherein R¹ and R² are each phenyl, C₁ -C₄ -alkylphenyl C₁ -C₄-alkoxyphenyl, 4-hydroxyphenyl, 2-thienyl or methyl, m is 1 or 2, R³ andR⁴ are each ##STR70## and one of the 4 radicals R³ and R⁴ mayfurthermore be phenyl, the radicals R¹⁰ independently of one another areeach C₁ -C₄ -alkyl and q is 1 or
 2. 4. The pigment as claimed in claim2, wherein F is a dye cation of the formula: ##STR71## wherein R¹ and R²are each phenyl, C₁ -C₄ -alkylphenyl C₁ -C₄ -alkoxyphenyl,4-hydroxyphenyl, 2-thienyl or methyl, m is 1 or 2, R³ and R⁴ are each##STR72## and one of the 4 radicals R³ and R⁴ may furthermore be phenyl,the radicals R¹⁰ independently of one another are each C₁ -C₄ -alkyl andq is 1 or
 2. 5. The pigment as claimed in claim 1, wherein F is a dyecation of the formula: ##STR73## wherein R⁸ is hydrogen, C₁ -C₄ -alkylor C₁ -C₄ -alkoxy, R⁹ is C₁ -C₄ -alkyl.
 6. The pigment is claimed inclaim 5, wherein, in the formulae, R⁸ is hydrogen, methyl, methoxy orhydroxyl, and N(R⁹)₂ is dimethylamino or diethylamino.
 7. The pigment asclaimed in claim 2, wherein F is a dye cation of the formula: ##STR74##wherein R⁸ is hydrogen, C₁ -C₄ -alkyl or C₁ -C₄ -alkoxy, and R⁹ is C₁-C₄ -alkyl.
 8. The pigment as claimed in claim 7, wherein, in theformulae R⁸ is hydrogen, methyl, methoxy or hydroxyl, and N(R⁹)₂ isdimethylamino or diethylamino.